美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=ORUDIS"
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商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
ORUDIS 018754 001 NDA KETOPROFEN CAPSULE;ORAL 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1986/01/09 1987/07/31 WYETH AYERST Discontinued
ORUDIS 018754 002 NDA KETOPROFEN CAPSULE;ORAL 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1986/01/09 1986/01/09 WYETH AYERST Discontinued
ORUDIS 018754 003 NDA KETOPROFEN CAPSULE;ORAL 75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1986/01/09 1986/01/09 WYETH AYERST Discontinued
ORUDIS KT 020429 001 NDA KETOPROFEN TABLET;ORAL 12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1995/10/06 1995/10/06 WYETH CONS Discontinued
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